EP1333027B1 - Production method of insecticidal and/or acaricidal ether compounds and intermediates thereof - Google Patents

Production method of insecticidal and/or acaricidal ether compounds and intermediates thereof Download PDF

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Publication number
EP1333027B1
EP1333027B1 EP03001125A EP03001125A EP1333027B1 EP 1333027 B1 EP1333027 B1 EP 1333027B1 EP 03001125 A EP03001125 A EP 03001125A EP 03001125 A EP03001125 A EP 03001125A EP 1333027 B1 EP1333027 B1 EP 1333027B1
Authority
EP
European Patent Office
Prior art keywords
formula
production method
water
given
ether compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP03001125A
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German (de)
English (en)
French (fr)
Other versions
EP1333027A1 (en
Inventor
Hiroshi Sakaguchi
Masaki Sasaki
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Chemical Co Ltd
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Sumitomo Chemical Co Ltd
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Filing date
Publication date
Application filed by Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Publication of EP1333027A1 publication Critical patent/EP1333027A1/en
Application granted granted Critical
Publication of EP1333027B1 publication Critical patent/EP1333027B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/63—One oxygen atom
    • C07D213/64—One oxygen atom attached in position 2 or 6
    • C07D213/643—2-Phenoxypyridines; Derivatives thereof

Definitions

  • the present invention relates to a production method of ether compounds which are useful as active ingredients of insecticide/acaricide or production intermediates thereof.
  • the publication also concretely discloses a production method of 1-benzyloxy-3,5-dichloro-4-[3-(5-trifluoromethylpyridin-2-yloxy)propoxy] benzene (the compound given by above formula (2) wherein R 2 is a hydrogen atom) by making 3-(2,6-dichloro-4-benzyloxy)phenoxy-1-propyl alcohol react with 2-chloro-5-trifluoromethylpyridine in the presence of a base in N,N-dimethylformamide.
  • the object of the present invention is to provide a production method of the ether compounds given by formula (3): wherein R 1 represents a benzyl group optionally substituted with a halogen atom(s) or 3,3-dihalo-2-propenyl group and R 2 represents a hydrogen atom or halogen atom, in high yield by using a hydrocarbon compound that is industrially available as a solvent.
  • the ether compound given by formula (3) can be produced by making the alcohol compounds given by formula (4): wherein R 1 represents a benzyl group optionally substituted with a halogen atom(s) or 3,3-dihalo-2-propenyl group, react with the pyridine compounds given by formula (5): wherein R 2 represents a hydrogen atom or halogen atom, in a hydrocarbon compound in the presence of alkali hydroxide or alkaline earth hydroxide with distilling off water from the reaction mixture in high yield and good quality.
  • the benzyl group optionally substituted with a halogen atom(s) for R 1 means a benzyl group or a benzyl group whose hydrogen atom(s) on the benzene ring is/are substituted with at least one halogen atom.
  • Typical examples include benzyl group and 4-chlorobenzyl group.
  • Examples of the 3,3-dihalo-2-propenyl group for R 1 include 3,3-dichloro-2-propenyl group and 3,3-dibromo-2-propenyl group.
  • halogen atom for R 2 examples include chlorine atom.
  • the production method of the present invention is characterized by making the alcohol compound given by formula (4) react with the pyridine compound given by formula (5) in a hydrocarbon compound in the presence of an alkali hydroxide or alkaline earth hydroxide with distilling off water.
  • the reaction is carried out in a hydrocarbon compound.
  • the hydrocarbon compound used for the reaction include aliphatic hydrocarbon compounds such as hexane, heptane, octane, nonane, decane, 3-methylpentane, cyclohexane, methylcyclohexane, ethylcyclohexane and so on; and aromatic hydrocarbon compounds such as toluene, xylene, mesitylene, ethylbenzene and so on.
  • hexane or heptane is used as the hydrocarbon compound.
  • the amount of the hydrocarbon compound used for the reaction is usually 0.3 to 50 parts by weight based on 1 part by weight of the alcohol compound given by formula (4), preferably 10 parts by weight or less in the view of the reaction rate.
  • the ratio of the alcohol compound given by formula (4) to the pyridine compound given by formula (5) used for the reaction is usually 0.9 to 2 mols of the pyridine compound given by formula (5) based to 1 mol of the alcohol compound given by formula (4).
  • alkali hydroxide and alkaline earth hydroxide used for the reaction examples include lithium hydroxide, sodium hydroxide, potassium hydroxide, calcium hydroxide and barium hydroxide.
  • the amount can be varied so long as the reaction proceeds, and it is usually 0.9 mol or more based on 1 mol of the alcohol compound given by formula (4) and 1.2 mols or less based on 1 mol of the pyridine compound given by formula (5).
  • the alkali hydroxide and alkaline earth hydroxide used for the reaction can be added to the reaction mixture as an aqueous solution.
  • the reaction temperature is in the range of 50 to 200°C and the reaction can be carried out under reduced pressure so that water can be easily distilled off from the reaction mixture.
  • the distillation of water is performed while the reaction is proceeding.
  • the method for distilling off water from the reaction mixture is, for example, 1) performing the reaction at the boiling point of water or more under normal pressure or reduced pressure and distilling off water from the reaction mixture or 2) performing the reaction at the boiling point of the solvent or more under normal pressure or reduced pressure and distilling off water together with the solvent from the reaction mixture.
  • the solvent can be recycled by using Dean-Stark water-separator and separating the solvent from water in the distillate.
  • the reaction can be carried out as follows.
  • the proceeding status of the reaction can be confirmed by analyzing the reaction product with chromatography such as high performance liquid chromatography and the like.
  • the ether compound given by formula (3) can be isolated by work-up procedures, for example, adding water to the reaction mixture, extracting with an organic solvent and concentrating the obtained organic layer.
  • the ether compound given by formula (6): wherein R 2 represents a hydrogen atom or halogen atom and R 4 represents a benzyl group optionally substituted with a halogen atom(s), which can be manufactured by the production method of the present invention, can be lead to a dihalopropene compound given by formula (7): wherein R 2 represents a hydrogen atom or halogen atom and R 5 represents a 3,3-dihalo-2-propenyl group, for example, according to the method described in USP-5,922,880.
  • the alcohol compound given by formula (4) can be prepared by the method disclosed in USP-5,922,880 or according to the description of USP-5,922,880.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
EP03001125A 2002-01-25 2003-01-20 Production method of insecticidal and/or acaricidal ether compounds and intermediates thereof Expired - Lifetime EP1333027B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2002016613A JP4154896B2 (ja) 2002-01-25 2002-01-25 エーテル化合物の製造法
JP2002016613 2002-01-25

Publications (2)

Publication Number Publication Date
EP1333027A1 EP1333027A1 (en) 2003-08-06
EP1333027B1 true EP1333027B1 (en) 2004-09-29

Family

ID=19192010

Family Applications (1)

Application Number Title Priority Date Filing Date
EP03001125A Expired - Lifetime EP1333027B1 (en) 2002-01-25 2003-01-20 Production method of insecticidal and/or acaricidal ether compounds and intermediates thereof

Country Status (13)

Country Link
US (1) US6590104B1 (zh)
EP (1) EP1333027B1 (zh)
JP (1) JP4154896B2 (zh)
CN (1) CN1234689C (zh)
AT (1) ATE277904T1 (zh)
AU (1) AU2003200192B2 (zh)
BR (1) BR0302681B1 (zh)
CA (1) CA2416811C (zh)
DE (1) DE60300057T2 (zh)
DK (1) DK1333027T3 (zh)
ES (1) ES2227488T3 (zh)
IL (1) IL153962A (zh)
ZA (1) ZA200300598B (zh)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101863828B (zh) * 2009-04-14 2012-01-11 中国中化股份有限公司 一种3，5，6-三卤代吡啶基醚类化合物及其应用
CN116178249B (zh) * 2023-02-22 2024-02-09 北京亦农生物科技有限公司 具有杀虫、杀螨活性的醚衍生物及其制备方法与应用

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK0722430T3 (da) 1994-08-04 1999-06-28 Sumitomo Chemical Co Dihalogenpropenforbindelser, insekticide/acaricide midler indeholdende samme og mellemprodukter til fremstilling deraf
TW307746B (zh) * 1994-10-14 1997-06-11 Sumitomo Chemical Co

Also Published As

Publication number Publication date
CA2416811A1 (en) 2003-07-25
CN1234689C (zh) 2006-01-04
JP2003221383A (ja) 2003-08-05
IL153962A (en) 2008-03-20
JP4154896B2 (ja) 2008-09-24
EP1333027A1 (en) 2003-08-06
ES2227488T3 (es) 2005-04-01
DK1333027T3 (da) 2004-10-25
BR0302681B1 (pt) 2013-12-31
CA2416811C (en) 2009-09-08
IL153962A0 (en) 2003-07-31
ATE277904T1 (de) 2004-10-15
DE60300057T2 (de) 2005-10-06
AU2003200192A1 (en) 2003-08-14
BR0302681A (pt) 2004-08-24
ZA200300598B (en) 2003-08-22
CN1434038A (zh) 2003-08-06
DE60300057D1 (de) 2004-11-04
US6590104B1 (en) 2003-07-08
AU2003200192B2 (en) 2008-01-10

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